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CS.[Na]

CSCc1ccc(C(=O)c2ccc(Cl)cc2)cc1
Reaction #2195
desired product
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1cc(OCc2ccccc2)c(SC(C)(C)C)cn1
Reaction #43437
(5-[(1,1-Dimethylethyl)thio]-4-[(phenylmethyl)oxy]-2-pyridinyl}methyl acetate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50383
compound XI
DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(-c2ccc(C(F)(F)F)cc2)ccc1C#N
Reaction #53576
2-methylthio-4-(4-trifluoromethylphenyl)benzonitrile
Ausbeute 75.4%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(C#N)=C1Sc2cn[nH]c(=O)c2S1
Reaction #54213
4,5-Dihydro-4-oxo-1,3-dithiolo (4,5-d)-pyridazine-2-ylidene-propanedinitrile
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1=C(C#N)Sc2c(cn[nH]c2=O)S1
Reaction #54681
5,6-Dihydro-5-oxo-1,4-dithiino(2,3-d)-pyridazine-2,3-dicarbonitrile
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(Sc3nc(-c4ccncc4)cs3)CS[C@H]12
Reaction #56683
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2COC3(CCCC3)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59905
title compound
Ausbeute 8.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2COC3(CCC3)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59906
title compound
Ausbeute 6.2%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)OCC(COc2ccnc(CS(=O)c3nc4ccccc4[nH]3)c2C)CO1.[Na]
Reaction #59908
title compound
Ausbeute 9.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2COC3(CCCCC3)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59912
title compound
Ausbeute 8.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OC2COC(C)(C)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59913
title compound
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OC2CCC3(CC2)OCCO3)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59914
title compound
Ausbeute 7.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCCC2COC(C)(C)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59916
title compound
Ausbeute 2.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCCC2(C)OCCCO2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59918
title compound
Ausbeute 2.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2OCCCO2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59920
title compound
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2(C)OCCCO2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59922
title compound
Ausbeute 8.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCCC2(C)OCC(C)(C)CO2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59924
title compound
Ausbeute 7.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCCC2(C)OCC3(CC3)CO2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59926
title compound
Ausbeute 5.5%DOI: 10.6084/m9.figshare.5104873.v1
COCC1(CCOc2ccnc(CS(=O)c3nc4ccccc4[nH]3)c2C)OCCCO1.[Na]
Reaction #59928
title compound
Ausbeute 7.0%DOI: 10.6084/m9.figshare.5104873.v1
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